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Evaluation of tool-like receptor-2 and 4 and interleukin-6 gene expressions in Turkish rheumatoid arthritis patients

Clinical rheumatology, 2016-11, Vol.35 (11), p.2693-2697

2016

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Mineralocorticoid receptor gene-2G/C polymorphism in central serous chorioretinopathy and relation of polymorphism with plasma cortisol levels

Guo ji yan ke za zhi, 2016-07, Vol.16 (7), p.1203-1206

2016

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Increased Expression of Matrix Metalloproteinases in Ligamentum Flavum Hypertrophy of the Patients with Lumbar Spinal Stenosis

International journal of human genetics, 2016-02, Vol.16 (1-2)

Eser, Betul

2016

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Intracerebral Hematoma Complicated With Brain Abscess in an Infant: Case Report

Neurologia medico-chirurgica, 2008, Vol.48(4), pp.176-178

2008

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The Effects of Polymorphisms of Death Pathway Genes and Mitochondrial Pathway Genes in Intervertebral Disc Degeneration

Turkish neurosurgery, 2017, Vol.27 (5), p.809-815

2017

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NUCB2 gene polymorphism and its relationship with nesfatin-1 levels in polycystic ovary syndrome

Gynecological endocrinology, 2016-01, Vol.32 (1), p.46-50

2016

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The prevalence of 4G/5G polymorphism of plasminogen activator inhibitor-1 (PAI-1) gene in central serous chorioretinopathy and its association with plasma PAI-1 levels

Cutaneous and ocular toxicology, 2014-12, Vol.33 (4), p.270-274

2014

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Association of the polymorphisms of vitamin D receptor and aggrecan genes with degenerative disc disease

Genetic testing and molecular biomarkers, 2010-06, Vol.14 (3), p.313

2010

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Two different nucleotide substitutions of APC gene in a family with familial adenomatous polyposis

Journal of surgical case reports, 2015-09, Vol.2015 (9), p.rjv118

2015

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The effects of IL-1A and IL-6 genes polymorphisms on gene expressions, hormonal and biochemical parameters in polycystic ovary syndrome

Journal of obstetrics and gynaecology, 2017-04, Vol.37 (3), p.358-362

2017

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Increased Expression of Matrix Metalloproteinases in Ligamentum Flavum Hypertrophy of the Patients with Lumbar Spinal Stenosis

International journal of human genetics, 2016-03, Vol.16 (1-2), p.1-9

2016

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Analysis of familial Mediterranean fever gene mutations in 202 patients with familial Mediterranean fever

Genetic testing, 2008-09, Vol.12 (3), p.341

2008

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CSCR 中盐皮质激素受体基因-2G/C 的多态性及其与血浆皮质醇水平的关系

国际眼科杂志, 2016, Vol.16 (7), p.1203-1206

2016

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CSCR中盐皮质激素受体基因-2G/C的多态性及其与血浆皮质醇水平的关系（英文）

国际眼科杂志, 2016, Vol.16 (7), p.1203-1206

Alper Yazici Esin Sogutlu Sari Betul Eser Gozde Sahin Medine Alpdemir Adil Kilic Muhammet Kazim Erol Sitki Samet Ermis

2016

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DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY

European journal of general medicine, 2011-12

2011

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Genotyping for Cx26 and Cx30 mutations in cases with congenital hearing loss

Genetic testing, 2008-06, Vol.12 (2), p.253

2008

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Osmanlı Câmi Mimârisinde Mükebbire

Eser, Betül

2019

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677C>T and 1298A>C polymorphisms of methylenetetrahydropholate reductase gene and biochemical parameters in Turkish population with spina bifida occulta

Turkish neurosurgery, 2010-01, Vol.20 (1), p.9-15

2010

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Intracerebral Hematoma Complicated With Brain Abscess in an Infant -Case Report

Neurologia medico-chirurgica, 2008, Vol.48 (4), p.176-178

2008

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Two different nucleotide substitutions of APC gene in a family with familial adenomatous polyposis

Journal of surgical case reports, 2015, Vol.2015 (9)

2015

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The effects of IL-1A and IL-6 genes polymorphisms on gene expressions, hormonal and biochemical parameters in polycystic ovary syndrome

Journal of the Turkish German Gynecological Association, 2016-05, Vol.17, p.S10

2016

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Mental health and psychological resilience among acne vulgaris patients during the pandemic: A cross‐sectional controlled study

Journal of cosmetic dermatology, 2021-12, Vol.20 (12), p.3739-3746

2021

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Post‐COVID syndrome: A single‐center questionnaire study on 1007 participants recovered from COVID‐19

Journal of medical virology, 2021-12, Vol.93 (12), p.6566-6574

2021

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Bioethical issues in genome editing by CRISPR-Cas9 technology

Turkish journal of biology, 2020-01, Vol.44 (2), p.110-120

2020

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Double-Blind Comparison of Ultrasonic and Conventional Osteotomy in Terms of Early Postoperative Edema and Ecchymosis

Aesthetic surgery journal, 2016-04, Vol.36 (4), p.390-401

2016

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Evaluation of tool-like receptor-2 and 4 and interleukin-6 gene expressions in Turkish rheumatoid arthritis patients

Mineralocorticoid receptor gene-2G/C polymorphism in central serous chorioretinopathy and relation of polymorphism with plasma cortisol levels

Increased Expression of Matrix Metalloproteinases in Ligamentum Flavum Hypertrophy of the Patients with Lumbar Spinal Stenosis

Intracerebral Hematoma Complicated With Brain Abscess in an Infant: Case Report

The Effects of Polymorphisms of Death Pathway Genes and Mitochondrial Pathway Genes in Intervertebral Disc Degeneration

NUCB2 gene polymorphism and its relationship with nesfatin-1 levels in polycystic ovary syndrome

The prevalence of 4G/5G polymorphism of plasminogen activator inhibitor-1 (PAI-1) gene in central serous chorioretinopathy and its association with plasma PAI-1 levels

Association of the polymorphisms of vitamin D receptor and aggrecan genes with degenerative disc disease

Two different nucleotide substitutions of APC gene in a family with familial adenomatous polyposis

The effects of IL-1A and IL-6 genes polymorphisms on gene expressions, hormonal and biochemical parameters in polycystic ovary syndrome

Increased Expression of Matrix Metalloproteinases in Ligamentum Flavum Hypertrophy of the Patients with Lumbar Spinal Stenosis

Analysis of familial Mediterranean fever gene mutations in 202 patients with familial Mediterranean fever

CSCR 中盐皮质激素受体基因-2G/C 的多态性及其与血浆皮质醇水平的关系

CSCR中盐皮质激素受体基因-2G/C的多态性及其与血浆皮质醇水平的关系（英文）

DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY

Genotyping for Cx26 and Cx30 mutations in cases with congenital hearing loss

Osmanlı Câmi Mimârisinde Mükebbire

677C>T and 1298A>C polymorphisms of methylenetetrahydropholate reductase gene and biochemical parameters in Turkish population with spina bifida occulta

Intracerebral Hematoma Complicated With Brain Abscess in an Infant -Case Report

Two different nucleotide substitutions of APC gene in a family with familial adenomatous polyposis

The effects of IL-1A and IL-6 genes polymorphisms on gene expressions, hormonal and biochemical parameters in polycystic ovary syndrome

Mental health and psychological resilience among acne vulgaris patients during the pandemic: A cross‐sectional controlled study

Post‐COVID syndrome: A single‐center questionnaire study on 1007 participants recovered from COVID‐19

Bioethical issues in genome editing by CRISPR-Cas9 technology

Double-Blind Comparison of Ultrasonic and Conventional Osteotomy in Terms of Early Postoperative Edema and Ecchymosis

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